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논문 기본 정보

자료유형
학술저널
저자정보
Cho, Man-Ho (Graduate School of Biotechnology, Kyung Hee University) Park, Hye Lin (Graduate School of Biotechnology, Kyung Hee University) Park, Jong-Hwa (Graduate School of Biotechnology, Kyung Hee University) Lee, Sang-Won (Department of Plant Molecular Systems Biotech and Crop Biotech Institute, Kyung Hee University) Bhoo, Seong Hee (Graduate School of Biotechnology, Kyung Hee University) Hahn, Tae-Ryong (Graduate School of Biotechnology, Kyung Hee University)
저널정보
한국응용생명화학회 Applied Biological Chemistry Applied Biological Chemistry 제55권 제6호
발행연도
2012.1
수록면
749 - 755 (7page)

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Flavonoids are ubiquitous secondary metabolites in plants and possess a wide range of biological activities such as anti-oxidant, anti-microbial, and anti-cancer activities. As a food ingredient, flavonoids are also thought to have health-promoting and disease-preventing properties. Structural modifications of flavonoids can improve their biological activities. Methylation is a common flavonoid modification that is catalyzed by O-methyltransferases (OMTs). We isolated four putative OMTs from the miniature tomato cultivar Micro-Tom. One OMT (SlOMT3) was successfully expressed in E. coli and purified. Recombinant SlOMT3 was found to be a regiospecific flavonoid 3'/5'-O-methyltransferase. Biochemical parameters show that SlOMT3 has higher binding affinity and catalytic efficiency for quercetin and luteolin than for eriodictyol. This suggests that flavonols and flavones are preferable substrates for SlOMT3. Biotransformation is considered a promising method to modify flavonoid structures. Transgenic E. coli expressing SlOMT3 was used to modify flavonoid substrates and was found to efficiently convert quercetin, luteolin, and eriodictyol to isorhamnetin, chrysoeriol and homoeriodictyol, respectively.

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